Results 321 to 330 of about 1,274,518 (371)

Correction to 'Chromosomal integrons are genetically and functionally isolated units of genomes'. [PDF]

Nucleic Acids Res
europepmc   +1 more source

Chromosomal Abnormalities in Miscarriages and Maternal Age: New Insights from the Study of 7118 Cases. [PDF]

Cells
Pendina AA, Krapivin MI, Chiryaeva OG, Petrova LI, Pashkova EP, Golubeva AV, Tikhonov AV, Koltsova AS, Trusova ED, Staroverov DA, Glotov AS, Bespalova ON, Efimova OA.   +12 more
europepmc   +1 more source

Influence of the Sex of Translocation Carrier on Clinical Outcomes of Couples Undergoing Preimplantation Genetic Testing. [PDF]

Mol Genet Genomic Med
Zhang Z, Chen J, Zhang L, Wei R, Liu Z, Zhao D, Bi X, Liang L, Zhang X, Su D, Wu X.   +10 more
europepmc   +1 more source

Recruitment and rejoining of remote double-strand DNA breaks for enhanced and precise chromosome editing. [PDF]

Genome Biol
Wang M, Fu P, Chen Z, Wang X, Ma H, Zhang X, Gao G.   +6 more
europepmc   +1 more source

Integrative cytogenetic and molecular studies unmask "chromosomal mimicry" in hematologic malignancies. [PDF]

Blood Adv
Zhao M, Ryall S, Brody SJ, Harris AC, Cabral K, Brownstein C, Kim JC, Smith AC, Dal Cin P, Narayan R, Sikkink K, Schmitt A, Hobbs GS, Fathi AT, Griffin GK, Sait SNJ, Iafrate AJ, Aster JC, Graubert TA, Nardi V, Dubuc AM.   +20 more
europepmc   +1 more source

Evaluation of prenatal and postnatal outcomes of fetuses with intrauterine cardiac anomalies: Tertiary center experience. [PDF]

Turk J Obstet Gynecol
Yılmaz GM, Demir SC, Aykut S, Evrüke İC, Sucu M.   +4 more
europepmc   +1 more source

Rapid Identification of Alien Chromosome Fragments and Tracing of Bioactive Compound Genes in Intergeneric Hybrid Offspring Between <i>Brassica napus</i> and <i>Isatis indigotica</i> Based on AMAC Method. [PDF]

Int J Mol Sci
Guo Y, Han Y, Gao J, Ge X, Luo Y, Zhao K, Li G, Zu F, Cheng X.   +8 more
europepmc   +1 more source

Prenatal diagnosis following preimplantation genetic testing (PGT): recommendations of the Italian Society of Human Genetics (SIGU). [PDF]

J Assist Reprod Genet
Grati FR, Capalbo A, Gabbiato I, Battaglia P, Pittalis MC, Bizzoco D, Cardarelli L, Gatta V, Lonardo F, Novelli A, Bernardini L, Zuccarello D, Italian Society of Human Genetics (SIGU).   +12 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Screening for Fetal Chromosomal Abnormalities.

Obstetrics and Gynecology, 2020
Prenatal testing for chromosomal abnormalities is designed to provide an accurate assessment of a patient's risk of carrying a fetus with a chromosomal disorder. A wide variety of prenatal screening and diagnostic tests are available; each offers varying
N. Rose, A. Kaimal, L. Dugoff, M. Norton
semanticscholar   +1 more source

Chromosome imprinting and the mammalian X chromosome [PDF]

Nature, 1975
Chromosome imprinting is the process by which one of two genetically homologous chromosomes is predetermined to function differently from the other at a subsequent stage in development. In the coccid insects, imprinting occurs in the egg, at the time of fertilisation; it probably occurs at the same time and site in mammals, and possibly also in Sciara.
Spencer W. Brown, H. Sharat Chandra
openaire   +2 more sources